Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626928Generated: November 1, 2026

Bromomethylcyclopropane → 5-Bromo-1-(cyclopropylmethyl)-1,2-dihydropyridin-2-one

https://huagongshe.com/reaction/1626928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethylcyclopropaneHCID 81503—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178515818HCID 178515818—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-1-(cyclopropylmethyl)-1,2-dihydropyridin-2-oneHCID 59635701—

Reaction Steps

To a solution of 5-bromopyridin-2-ol (1.0 g, 5.75 mmol) in DMF (10 mL) at RT, potassium tert-butoxide (0.68 g, 6.07 mmol) was added and the mixture was stirred for 30 min. To this mixture, (bromomethyl)cyclopropane (1.03 g, 8.62 mmol) was added, and the resulting mixture was stirred at 70° C. for 2 h. The mixture was allowed to cool to RT, diluted with EtOAc (50 mL) and quenched with water (20 mL). The organic layer was washed with water (2×20 mL) and brine (20 mL), dried over anhydrous MgSO4 and filtered. The filtrate was concentrated in vacuo to afford 5-bromo-1-(cyclopropylmethyl)pyridin-2(1H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785470B2
Source datasetuspto-grants-2014_07
ORD IDord-49cd24bfa3e24a0db496b2a74d60aa83
Source noteuspto-grants-2014_07